Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523911 | 7235221 | I | 6523911-X | 20091202 | 20091223 | 20091231 | EXP | NL-ABBOTT-09P-114-0616187-00 | ABBOTT LABORATORIES | 32 | M | Y | 20091231 | NETHERLANDS |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523911 | 1012888026 | PS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 6523911 | 1012888027 | C | ZYPREXA | 1 | ORAL | ||||||
| 6523911 | 1012888028 | C | AKINETON | 1 | ORAL | ||||||
| 6523911 | 1012888029 | C | ARTHROTEC | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523911 | 1012888026 | SWEAT GLAND INFECTION |
| 6523911 | 1012888027 | DRUG USE FOR UNKNOWN INDICATION |
| 6523911 | 1012888028 | DRUG USE FOR UNKNOWN INDICATION |
| 6523911 | 1012888029 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523911 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6523911 | PSYCHOTIC DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6523911 | 1012888026 | 20090820 |